Regional Medical Director overseeing clinical strategy for Crossover Health in the Bay Area. Focus on improving patient engagement, quality, and overall health services strategy.
About the role
- Global Medical Director responsible for implementing medical strategies globally for Cell & Gene Therapy in Oncology. Leading evidence generation activities and representing Global Medical Affairs with stakeholders.
Responsibilities
- Lead development and execution of medical affairs strategy for Oncology Cell & Gene priority programs including transformative tactics such as: research/population health, innovative partnerships and integrated evidence plans
- Co-develop plans for evidence generation, Medical Science Liaison (MSL) / Field Medical Affairs strategy, medical education programs, scientific publication planning and Medical Expert network development with (TAs)
- Co-own the development and implementation of innovative education and scientific communication plans for external stakeholders
- Financial tracking to ensure timely and cost-effective development & execution of medical activities
- Prepare Scientific Review Committee submissions for TA assets within remit
- Partner with Development, Strategy and growth (S&G), US and International cross-functions to shape portfolio early and diversify evidence to achieve broad access at launch and to enhance impact on clinical practice for priority programs
- Represent GMA around prioritized portfolio with internal and external audiences, in collaboration with TAs including the investment, medical and regulatory communities, as well as pharmaceutical or biotechnology industry collaborators/partners
- Represent “the voice of the patient” internally and evaluate factors relevant to a patient’s informed decision making
- Provide direction and input into the development and implementation of successful reimbursement and market-access strategies
- Provide proactive input to Development on potential new therapeutic indications, to enrich Registration Programs and to consider new therapeutic opportunities.
- Ensure that Patient Access programs are supported for all brands within the GMA and delivered with full compliance
- Ensures GMA activities are designed and executed in compliance with company policy guidelines and highest medical quality standards
- Provide proactive medical input to asset lifecycle management to consider new therapeutic opportunities
Requirements
- MD (Preferred) or PhD/PharmD in Health Sciences.
- 5+ years in Pharmaceutical Industry experience in Medical Affairs and/or Clinical Development
- Firm working knowledge of GCP, scientific and clinical methodology, protocol designs, management and regulatory requirements for clinical studies designated for review by regulatory authorities.
- Strategic mindset and able to establish credibility and influence across a range of diverse stakeholders in a matrix organization to drive change with an agile mindset & ability to lead in an agile organization across Disease Areas
- Ability to truly collaborate across functions and markets: serve-partner-co-create
- Deep understanding of health care systems and key external stakeholders
- Strong track record of delivery focus for time and quality in medical affairs projects with successful development and implementation of innovative programs and processes
- Understands unmet medical needs, generates the right evidence to fulfil them, uses innovative, multichannel communication formats for effective evidence dissemination.
Benefits
- Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Tech skills
Location requirements
Clinical Director responsible for administration and clinical operations at a Comprehensive Health Center, ensuring compliance and quality of care.
Medical Director leading clinical initiatives and supporting healthcare policies in UK insurance. Collaborating with industry leaders and managing healthcare practices to ensure quality care.
Global Medical Director developing and executing medical plans for Urothelial Cancer at Pfizer. Collaborating with cross - functional teams to advance communication and clinical trial execution.
Medical Director/Senior Director leading clinical development at Scholar Rock, focusing on late - stage product candidates. Ensuring robust scientific and medical leadership from proof - of - concept to marketing approval.
Global Medical Director leading medical strategy execution for Rare Hematology products at Sanofi. Driving evidence generation and expert outreach for critical healthcare advancements.
Regional Director of Clinical Operations for CommuniCare Health Services overseeing clinical policy compliance and managing nursing teams. Requires extensive experience in Long Term Care and Nursing Consulting.
Clinical Director overseeing clinical operations and staff in Washburn's 32 bed Detoxification program. Collaborating with leadership to enhance staff education and programming standards.
Center Medical Director at Oak Street Health leading clinical teams to provide excellent patient care. Focused on primary care practice and supporting provider growth with meaningful initiatives.
Critical leadership role at GSK ensuring alignment of oncology strategy and activities across Europe. Develop and build scientific expertise for better strategy and competitive engagement.